Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg1 |
C |
T |
17: 31,327,321 (GRCm39) |
R339C |
possibly damaging |
Het |
Adamts6 |
G |
A |
13: 104,565,436 (GRCm39) |
G721R |
probably damaging |
Het |
Adnp2 |
A |
G |
18: 80,171,274 (GRCm39) |
V1045A |
probably benign |
Het |
Agbl3 |
T |
C |
6: 34,823,888 (GRCm39) |
I856T |
probably benign |
Het |
Anapc1 |
T |
A |
2: 128,526,454 (GRCm39) |
K115* |
probably null |
Het |
Atp10a |
T |
C |
7: 58,447,562 (GRCm39) |
I768T |
possibly damaging |
Het |
Blk |
C |
T |
14: 63,622,375 (GRCm39) |
R55H |
probably benign |
Het |
Ccdc158 |
T |
C |
5: 92,810,005 (GRCm39) |
S168G |
probably benign |
Het |
Cda |
G |
T |
4: 138,066,253 (GRCm39) |
T128K |
probably benign |
Het |
Celsr1 |
T |
A |
15: 85,791,799 (GRCm39) |
T2601S |
probably damaging |
Het |
Dmxl1 |
T |
C |
18: 50,013,847 (GRCm39) |
V1545A |
possibly damaging |
Het |
Dst |
T |
A |
1: 34,309,971 (GRCm39) |
N6264K |
probably damaging |
Het |
Ednra |
T |
C |
8: 78,401,718 (GRCm39) |
S191G |
probably damaging |
Het |
Elk3 |
A |
T |
10: 93,100,912 (GRCm39) |
S280T |
possibly damaging |
Het |
Etnk1 |
A |
G |
6: 143,126,343 (GRCm39) |
I63V |
possibly damaging |
Het |
Fscb |
A |
G |
12: 64,518,347 (GRCm39) |
S1040P |
unknown |
Het |
Gm14295 |
T |
G |
2: 176,502,420 (GRCm39) |
C637G |
probably damaging |
Het |
Gm5114 |
T |
C |
7: 39,057,997 (GRCm39) |
T541A |
probably benign |
Het |
Man2c1 |
T |
C |
9: 57,042,849 (GRCm39) |
F240L |
probably benign |
Het |
Map2 |
A |
T |
1: 66,454,766 (GRCm39) |
I1219L |
probably benign |
Het |
Map3k13 |
A |
G |
16: 21,711,173 (GRCm39) |
Y152C |
probably damaging |
Het |
Morc1 |
G |
A |
16: 48,322,683 (GRCm39) |
A327T |
probably damaging |
Het |
Myo3a |
A |
T |
2: 22,366,475 (GRCm39) |
Y553F |
probably benign |
Het |
Myo9b |
T |
A |
8: 71,804,803 (GRCm39) |
|
probably null |
Het |
Or14j1 |
A |
C |
17: 38,146,694 (GRCm39) |
D268A |
probably damaging |
Het |
Or5b3 |
C |
T |
19: 13,387,957 (GRCm39) |
T8I |
probably damaging |
Het |
Pam |
A |
G |
1: 97,823,774 (GRCm39) |
V219A |
probably benign |
Het |
Panx1 |
A |
G |
9: 14,918,929 (GRCm39) |
I310T |
possibly damaging |
Het |
Pde6a |
T |
A |
18: 61,397,057 (GRCm39) |
F634L |
possibly damaging |
Het |
Pkd1l2 |
C |
A |
8: 117,757,370 (GRCm39) |
C1556F |
probably damaging |
Het |
Prdm5 |
G |
A |
6: 65,860,635 (GRCm39) |
V440I |
probably damaging |
Het |
Rasa2 |
T |
C |
9: 96,493,493 (GRCm39) |
T64A |
probably damaging |
Het |
Sec24b |
A |
T |
3: 129,834,881 (GRCm39) |
Y106N |
probably damaging |
Het |
Sfswap |
C |
T |
5: 129,627,883 (GRCm39) |
Q689* |
probably null |
Het |
Slamf8 |
C |
T |
1: 172,417,965 (GRCm39) |
|
probably null |
Het |
Tektl1 |
G |
A |
10: 78,588,726 (GRCm39) |
T28M |
probably benign |
Het |
Tmt1a3 |
A |
G |
15: 100,233,123 (GRCm39) |
K105E |
probably benign |
Het |
Tsr1 |
T |
C |
11: 74,799,177 (GRCm39) |
V786A |
probably benign |
Het |
Yod1 |
G |
A |
1: 130,645,275 (GRCm39) |
G19S |
probably damaging |
Het |
Zmynd10 |
T |
C |
9: 107,425,079 (GRCm39) |
I58T |
possibly damaging |
Het |
|
Other mutations in Arc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01778:Arc
|
APN |
15 |
74,544,204 (GRCm39) |
missense |
probably benign |
|
IGL02372:Arc
|
APN |
15 |
74,543,954 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03209:Arc
|
APN |
15 |
74,543,833 (GRCm39) |
missense |
probably damaging |
1.00 |
P0040:Arc
|
UTSW |
15 |
74,543,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R0732:Arc
|
UTSW |
15 |
74,543,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R1377:Arc
|
UTSW |
15 |
74,544,101 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2430:Arc
|
UTSW |
15 |
74,543,740 (GRCm39) |
missense |
probably benign |
0.01 |
R4647:Arc
|
UTSW |
15 |
74,543,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R4855:Arc
|
UTSW |
15 |
74,543,592 (GRCm39) |
missense |
probably benign |
0.01 |
R6436:Arc
|
UTSW |
15 |
74,544,098 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8678:Arc
|
UTSW |
15 |
74,543,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:Arc
|
UTSW |
15 |
74,543,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R9070:Arc
|
UTSW |
15 |
74,543,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9184:Arc
|
UTSW |
15 |
74,543,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R9428:Arc
|
UTSW |
15 |
74,543,063 (GRCm39) |
missense |
probably benign |
0.01 |
RF003:Arc
|
UTSW |
15 |
74,543,980 (GRCm39) |
missense |
probably benign |
0.00 |
|